Wang Xiaoru, Wang Yulin
Cell Physiol Biochem. 2015;37(2):641-50. doi: 10.1159/000430383.
BACKGROUND/AIMS: Acute myeloid leukemia (AML) is a severe malignant cancer worldwide, in both adult and pediatric patients. Since bone marrow cell transplantation is seriously limited by the availability of the immune-paired donor sources, the therapy for pediatric leukemia remains challenging. Ginsenoside Rh2 (GRh2) is a well-characterized component in red ginseng, and has established therapeutic effects for different diseases, although whether GRh2 may have a therapeutic effect on pediatric leukemia has not been investigated.
We examined the effects of GRh2 on the survival of mice in an acute leukemia model. We analyzed the effects of GRh2 on the cell viability of leukemia cell lines in vitro, using a CCK-8 assay and an MTT assay. We analyzed the effects of GRh2 on the apoptosis of leukemia cell lines in vitro, by flow cytometry. We analyzed the levels of Bcl-2 and microRNA-21 (miR-21) in GRh2-treated leukemia cells. Prediction of binding between miR-21 and 3'-UTR of Bcl-2 mRNA was performed by a bioinformatics algorithm and confirmed by a dual luciferase reporter assay.
GRh2 significantly prolonged the survival of mice with pediatric leukemia. GRh2 significantly decreased the viability of leukemia cells in vitro, through induction of apoptosis. GRh2 significantly decreased the levels of an anti-apoptotic protein Bcl-2 in leukemia cells, possibly through induction of miR-21, which suppressed the translation of Bcl-2 mRNA via 3'-UTR binding.
GRh2 may be an effective treatment for pediatric leukemia, and GRh2 may induce apoptosis of leukemia cells through miR-21-modulated suppression of Bcl-2.
背景/目的:急性髓系白血病(AML)是一种在全球范围内影响成人和儿童患者的严重恶性肿瘤。由于骨髓细胞移植严重受限于免疫配对供体来源的可用性,小儿白血病的治疗仍然具有挑战性。人参皂苷Rh2(GRh2)是红参中一种特性明确的成分,对不同疾病已证实具有治疗作用,尽管GRh2对小儿白血病是否具有治疗作用尚未得到研究。
我们在急性白血病模型中检测了GRh2对小鼠存活的影响。我们使用CCK-8法和MTT法在体外分析了GRh2对白血病细胞系细胞活力的影响。我们通过流式细胞术在体外分析了GRh2对白血病细胞系凋亡的影响。我们分析了GRh2处理的白血病细胞中Bcl-2和微小RNA-21(miR-21)的水平。通过生物信息学算法预测miR-21与Bcl-2 mRNA的3'-UTR之间的结合,并通过双荧光素酶报告基因检测进行验证。
GRh2显著延长了小儿白血病小鼠的存活时间。GRh2通过诱导凋亡在体外显著降低了白血病细胞的活力。GRh2可能通过诱导miR-21显著降低白血病细胞中抗凋亡蛋白Bcl-2的水平,miR-21通过与3'-UTR结合抑制Bcl-2 mRNA的翻译。
GRh2可能是小儿白血病的一种有效治疗方法,并且GRh2可能通过miR-21介导的对Bcl-2的抑制诱导白血病细胞凋亡。